134 Improvements in Clinical Global Impression of Change With Deutetrabenazine Treatment in Tardive Dyskinesia From the ARM-TD and AIM-TD Studies. (15th June 2018)
- Record Type:
- Journal Article
- Title:
- 134 Improvements in Clinical Global Impression of Change With Deutetrabenazine Treatment in Tardive Dyskinesia From the ARM-TD and AIM-TD Studies. (15th June 2018)
- Main Title:
- 134 Improvements in Clinical Global Impression of Change With Deutetrabenazine Treatment in Tardive Dyskinesia From the ARM-TD and AIM-TD Studies
- Authors:
- Fernandez, Hubert H.
Davis, Mat D.
Factor, Stewart A.
Hauser, Robert A.
Jarskog, L. Fredrik
Jimenez-Shahed, Joohi
Kumar, Rajeev
Ochudlo, Stanislaw
Ondo, William G.
Anderson, Karen E. - Abstract:
- Abstract: Introduction: Tardive dyskinesia (TD) is an involuntary movement disorder that is often irreversible, can affect any body region, and can be debilitating. In the ARM-TDand AIM-TD studies, deutetrabenazine treatment demonstrated statistically and clinically significant reductions in Abnormal Involuntary Movement Scale (AIMS) scores at Week 12 compared with placebo (primary endpoint). Objective: To evaluate the efficacy of deutetrabenazine, as measured by the Clinical Global Impression of Change (CGIC) scale, in patients with TD from the pooled ARM-TDand AIM-TD (24 and 36 mg/day doses) data sets, as compared with the pooled placebo cohort. Methods: ARM-TD and AIM-TD were 12-week, randomized, double-blind, placebo-controlled studies that evaluated the safety and efficacy of deutetrabenazine for thetreatment of TD. The key secondary endpoint of each study was the proportion of patients "much improved" or "very much improved" (treatment success) at Week 12 on theCGIC. Results: At Week 12, the odds of treatment success among patients treated with deutetrabenazine (n=152) was more than double that of patients given placebo (n=107; odds ratio: 2.12; P=0.005). In a categorical analysis of CGIC ratings, patients treated with deutetrabenazine showed greater improvement than patients given placebo (P=0.003). Patients treated with deutetrabenazine also had a significantly better treatment response than those given placebo (least-squares mean CGIC score treatment difference:Abstract: Introduction: Tardive dyskinesia (TD) is an involuntary movement disorder that is often irreversible, can affect any body region, and can be debilitating. In the ARM-TDand AIM-TD studies, deutetrabenazine treatment demonstrated statistically and clinically significant reductions in Abnormal Involuntary Movement Scale (AIMS) scores at Week 12 compared with placebo (primary endpoint). Objective: To evaluate the efficacy of deutetrabenazine, as measured by the Clinical Global Impression of Change (CGIC) scale, in patients with TD from the pooled ARM-TDand AIM-TD (24 and 36 mg/day doses) data sets, as compared with the pooled placebo cohort. Methods: ARM-TD and AIM-TD were 12-week, randomized, double-blind, placebo-controlled studies that evaluated the safety and efficacy of deutetrabenazine for thetreatment of TD. The key secondary endpoint of each study was the proportion of patients "much improved" or "very much improved" (treatment success) at Week 12 on theCGIC. Results: At Week 12, the odds of treatment success among patients treated with deutetrabenazine (n=152) was more than double that of patients given placebo (n=107; odds ratio: 2.12; P=0.005). In a categorical analysis of CGIC ratings, patients treated with deutetrabenazine showed greater improvement than patients given placebo (P=0.003). Patients treated with deutetrabenazine also had a significantly better treatment response than those given placebo (least-squares mean CGIC score treatment difference: –0.4; P=0.006). Conclusions: Deutetrabenazine treatment led to statistically and clinically significant improvements in TD symptoms based on the CGIC result, suggesting that clinicians were able to recognize the benefit in patients treated with deutetrabenazine. Presented at: The International Congress of Parkinson's Disease and Movement Disorders; June 4–8, 2017; Vancouver, British Columbia, Canada. Funding Acknowledgements: These studies were funded by Teva Pharmaceutical Industries, Petach Tikva, Israel. … (more)
- Is Part Of:
- CNS spectrums. Volume 23:Number 1(2018:Feb.)
- Journal:
- CNS spectrums
- Issue:
- Volume 23:Number 1(2018:Feb.)
- Issue Display:
- Volume 23, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 23
- Issue:
- 1
- Issue Sort Value:
- 2018-0023-0001-0000
- Page Start:
- 84
- Page End:
- 84
- Publication Date:
- 2018-06-15
- Subjects:
- Neuropsychiatry -- Periodicals
Nervous system -- Diseases -- Periodicals
Neurology -- Periodicals
616.8005 - Journal URLs:
- http://journals.cambridge.org/cns ↗
http://www.cnsspectrums.com ↗ - DOI:
- 10.1017/S1092852918000305 ↗
- Languages:
- English
- ISSNs:
- 1092-8529
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 10459.xml